The G2019S LRRK2 mutation is frequent in north African families with Parkinson's disease

被引：0
|
作者：
Lesage, S. [1 ]
Ibanez, P. [1 ]
Lohmann, E. [1 ,3 ]
Pollak, P. [5 ]
Tison, F. [6 ]
Tazir, M. [7 ]
Leutenegger, A. L. [1 ]
Guimaraes, J. [8 ]
Bonnet, A. M. [3 ]
Durr, A. [1 ,2 ,3 ]
Brice, A. [1 ,2 ,3 ,4 ]
机构：
[1] INSERM, U679, U289, F-75654 Paris 13, France
[2] Hop La Pitie Salpetriere, Dept Genet Cytogenet & Embryol, Paris, France
[3] Federat Neurol, Paris, France
[4] CHU Pitie Salpetriere, UFR, AP HP, Paris, France
[5] CHU Grenoble, Dept Neurol, F-38043 Grenoble, France
[6] CHU Bordeaux, Hop Haut Leveque, Serv Neurol, Pessac, France
[7] CHU Mustapha, Serv Neurol, Algiers, Algeria
[8] Hosp Egas Moniz, Serv Neurol, Lisbon, Portugal
来源：
EUROPEAN JOURNAL OF NEUROLOGY | 2005年 / 12卷
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D O I：
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中图分类号：
R74 [神经病学与精神病学];
学科分类号：
摘要：
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页码：31 / 32
页数：2
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